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Nele Hilgert

Showing results (1-10 of 15) with videos related to

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Human Genetics|October 11, 2008
Gene symbol: TMC1. Disease: Hearing lossNele Hilgert
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: GPR98. Disease: Usher syndrome 2CNele Hilgert
Human Genetics|October 11, 2008
Gene symbol: TMC1. Disease: DeafnessNele Hilgert
Current Molecular Medicine|July 16, 2009
Function and expression pattern of nonsyndromic deafness genesNele Hilgert, Richard J H Smith, Guy Van Camp
Mutation Research|September 23, 2008
Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?Nele Hilgert, Richard J H Smith, Guy Van Camp
European Journal of Human Genetics : EJHG|January 24, 2008
A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing lossNele Hilgert, Vedat Topsakal, Joost van Dinther, et al.
Journal of Human Genetics|January 31, 2009
Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairmentNele Hilgert, Kelly Monahan, Kiyoto Kurima, et al.
Audiology & Neuro-Otology|November 7, 2009
Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutationsVedat Topsakal, Nele Hilgert, Joost van Dinther, et al.
Biochimica Et Biophysica Acta|November 26, 2008
Are MYO1C and MYO1F associated with hearing loss?Cristina Zadro, Maria Stella Alemanno, Emanuele Bellacchio, et al.
Human Genetics|January 29, 2008
A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9Insaf Bel Hadj Ali, Melissa Thys, Najeh Beltaief, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Human Genetics|October 11, 2008
Gene symbol: TMC1. Disease: Hearing lossNele Hilgert
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: GPR98. Disease: Usher syndrome 2CNele Hilgert
Human Genetics|October 11, 2008
Gene symbol: TMC1. Disease: DeafnessNele Hilgert
Current Molecular Medicine|July 16, 2009
Function and expression pattern of nonsyndromic deafness genesNele Hilgert, Richard J H Smith, Guy Van Camp
Mutation Research|September 23, 2008
Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?Nele Hilgert, Richard J H Smith, Guy Van Camp
European Journal of Human Genetics : EJHG|January 24, 2008
A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing lossNele Hilgert, Vedat Topsakal, Joost van Dinther, et al.
Journal of Human Genetics|January 31, 2009
Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairmentNele Hilgert, Kelly Monahan, Kiyoto Kurima, et al.
Audiology & Neuro-Otology|November 7, 2009
Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutationsVedat Topsakal, Nele Hilgert, Joost van Dinther, et al.
Biochimica Et Biophysica Acta|November 26, 2008
Are MYO1C and MYO1F associated with hearing loss?Cristina Zadro, Maria Stella Alemanno, Emanuele Bellacchio, et al.
Human Genetics|January 29, 2008
A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9Insaf Bel Hadj Ali, Melissa Thys, Najeh Beltaief, et al.
Pageof 2